A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7843379



Internal ID13275774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1473946..1473946hg38UCSC Ensembl
chr10:1516141..1516141hg19UCSC Ensembl
chr10:1506141..1506141hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3310506
Supporting Variants
SamplesNA12878
Known GenesADARB2
MethodSequencing
AnalysisCortex de-novo
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7843379
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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